Canonical Allele Identifier: CA1433504784

Gene: FGFR3

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1801377C= , CM000666.2:g.1801377C=	GRCh38
NC_000004.11:g.1803104C= , CM000666.1:g.1803104C=	GRCh37
NC_000004.10:g.1772902C=	NCBI36
NG_012632.1:g.13066C= , LRG_1021:g.13066C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340107.9:c.456C=	ENSP00000339824.4:p.Tyr152=
ENST00000260795.8:c.456C=	ENSP00000260795.3:p.Tyr152=
ENST00000352904.6:c.456C=	ENSP00000231803.1:p.Tyr152=
ENST00000412135.7:c.444C=	ENSP00000412903.3:p.Tyr148=
ENST00000440486.8:c.456C= MANE Select	ENSP00000414914.2:p.Tyr152=
ENST00000481110.7:c.456C=	ENSP00000420533.2:p.Tyr152=
ENST00000260795.6:c.456C=	ENSP00000260795.2:p.Tyr152=
ENST00000340107.8:c.456C=	ENSP00000339824.4:p.Tyr152=
ENST00000352904.5:c.456C=	ENSP00000231803.1:p.Tyr152=
ENST00000412135.6:c.456C=	ENSP00000412903.2:p.Tyr152=
ENST00000440486.6:c.456C=	ENSP00000414914.2:p.Tyr152=
ENST00000481110.6:c.456C=	ENSP00000420533.2:p.Tyr152=
ENST00000613647.4:c.456C=	ENSP00000479472.1:p.Tyr152=
NM_000142.4:c.456C= , LRG_1021t1:c.456C=	NP_000133.1:p.Tyr152=
NM_001163213.1:c.456C= , LRG_1021t2:c.456C=	NP_001156685.1:p.Tyr152=
NM_022965.3:c.456C=	NP_075254.1:p.Tyr152=
XM_006713868.1:c.456C=	XP_006713931.1:p.Tyr152=
XM_006713869.1:c.456C=	XP_006713932.1:p.Tyr152=
XM_006713870.1:c.456C=	XP_006713933.1:p.Tyr152=
XM_006713871.1:c.456C=	XP_006713934.1:p.Tyr152=
XM_006713872.1:c.456C=	XP_006713935.1:p.Tyr152=
XM_006713873.1:c.456C=	XP_006713936.1:p.Tyr152=
XM_011513420.1:c.456C=	XP_011511722.1:p.Tyr152=
XM_011513422.1:c.456C=	XP_011511724.1:p.Tyr152=
NM_001354809.1:c.456C=	NP_001341738.1:p.Tyr152=
NM_001354810.1:c.456C=	NP_001341739.1:p.Tyr152=
NR_148971.1:n.712C=
NM_001354809.2:c.456C=	NP_001341738.1:p.Tyr152=
NM_001354810.2:c.456C=	NP_001341739.1:p.Tyr152=
NR_148971.2:n.731C=
NM_000142.5:c.456C= MANE Select	NP_000133.1:p.Tyr152=
NM_001163213.2:c.456C=	NP_001156685.1:p.Tyr152=
NM_022965.4:c.456C=	NP_075254.1:p.Tyr152=